{{Rsnum
|rsid=149428
|Chromosome=16
|position=58634662
|Orientation=plus
|GMAF=0.1983
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 11.5 | 50.4 | 38.1
| HCB | 0.7 | 10.2 | 89.1
| JPT | 0.0 | 2.7 | 97.3
| YRI | 2.0 | 17.7 | 80.3
| ASW | 3.5 | 29.8 | 66.7
| CHB | 0.7 | 10.2 | 89.1
| CHD | 0.0 | 8.3 | 91.7
| GIH | 3.0 | 31.7 | 65.3
| LWK | 0.0 | 10.9 | 89.1
| MEX | 0.0 | 43.1 | 56.9
| MKK | 0.0 | 16.0 | 84.0
| TSI | 9.8 | 52.0 | 38.2
| HapMapRevision=28
}}{{omim
|desc=SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35
|id=612319
|rsnum=149428
}}

{{PMID|18463364}} A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}